| Primary Identifier | MGI:1888971 | Organism | mouse, laboratory |
| Chromosome | 15 | NCBI Gene Number | 29859 |
| Mgi Type | protein coding gene |
| description | FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0) Enables sulfotransferase activity. Acts upstream of or within sulfur compound metabolic process. Located in cytosol and mitochondrion. Is expressed in embryo. Orthologous to human SULT4A1 (sulfotransferase family 4A member 1). PHENOTYPE: Mice homozygous for a null allele exhibit progressive tremors, ataxia, abnormal gait, absence seizure, porstnatal growth retardation and premature death. [provided by MGI curators] |
Features --> Cross References
Canonical gene --> CDSs in specific strains.
Canonical gene --> Exons in specific strains
Canonical gene --> Strain-specific IDs, biotypes, and locations
Canonical gene --> Transcripts in specific strains.
Features --> Overlapping features
